Catheter movement control

ABSTRACT

An endovascular device monitoring system is provided that determines, based on movement of the endovascular device past a selected reference location, at least one of a movement rate of a endovascular device and position of a distal end of a endovascular device in a body of a patient.

FIELD

The disclosure relates generally to endovascular devices andparticularly to monitoring the use of catheters.

BACKGROUND

Catheters are medical devices that can be inserted into a body cavity,duct, or vessel to treat diseases or perform a surgical procedure.Catheterization, for example, is performed in cardiovascular, urologicalgastrointestinal, neurovascular, and ophthalmic applications. Catheterscan allow drainage, administration of fluids or gases, access bysurgical instruments, and perform wide variety of other tasks dependingon the type of catheter. Catheters can, for instance, include energyemitting devices, such as laser and other radiation emitters, to ablateor cauterize tissue. In most uses, catheter is a thin, flexible tube(“soft” catheter) though catheters are available in varying levels ofstillness depending on the application.

Catheterization is normally performed in a series of steps. Anintroducer needle is first inserted into the body lumen followed byinsertion of a guide wire through the introducer needle and into thelumen. The inserted introducer needle is removed, and an introducersheath and/or dilator are introduced over the guide wire into thedesired position to hold the body lumen open and allow insertion oftools, such as the catheter. The catheter can be introduced through thelumen of the introducer sheath using the wire as a guide.

In many applications, the rate of advancement and/or removal ofcatheters is important not only to patient safety but also to optimalusage of the catheter. Some catheters require a narrow range ofadvancement rates for effective performance. Laser catheters, forexample, should be advanced at a rate of less than about 1 mm/second.Advancing too quickly can increase risk of injury (such as duringsuperior vena cava during lead extraction), increase the forces actingat the laser sheath tip, and prevent the laser from properly ablatingtissue (particularly with a smaller body lumen diameter with rapidcatheter advancement). Advancing too slowly and lasing tissue too longcan also provide poor results.

SUMMARY

These and other needs are addressed by the various aspects, embodiments,and configurations of the present disclosure. The disclosure is directedgenerally to an endovascular device monitoring system.

A method, according to this disclosure, can include the step ofdetermining, by a microprocessor executable controller and based onmovement of the endovascular device past a selected reference location,one or more of a movement rate of an endovascular device and position ofa distal end of an endovascular device in a body of a patient.

A non-transient, tangible computer readable medium or system, accordingto this disclosure, can include microprocessor executable controllerlogic that, when executed, determines, based on endovascular devicemovement past a selected reference location, endovascular devicemovement rate and/or endovascular device distal end or tip position.

The rate is commonly one or more of velocity and acceleration of anendovascular device component.

The controller can detect, by an endovascular device movement sensorpositioned at the selected reference location, displacement of one ormore markers associated with the endovascular device.

Endovascular device movement can be determined by any of a number oftechniques. Endovascular device movement, for example, can be based onone or more of rotation and displacement of a component mechanicallyengaged with a portion of the endovascular device; a variation inoptical property of light reflected by the markers moving past theselected reference location (the variation being caused by the markershaving an optical property different from that of other (intervening)parts of the endovascular device); a variation in magnetic fieldstrength along a length of the endovascular device body (the variationbeing caused by the markers having a magnetic property different fromthat of other (intervening) parts of the endovascular device); andreading a radio frequency parameter associated with the markers (whichcan be an active and/or passive Radio Frequency-IDentification (“RFID”)tag).

The endovascular device movement sensor can be positioned on or adjacentto an introducer sheath assembly and/or the endovascular device itself.

The endovascular device movement sensor can be positioned externally orinternally to the body of a patient.

When the controller determines that the endovascular device movementrate and/or distal end or tip position is unacceptable, the controllercan, via a user interface, notify a user of the unacceptable movementrate and/or distal end or tip position in the body of the patient.Alternatively or additionally, the controller can cause a microprocessorexecutable endovascular device parameter adjustment module to adjust anendovascular device parameter. The endovascular device parameter can,for instance, be one or more of endovascular device velocity,endovascular device acceleration, endovascular device speed,endovascular device operational state, endovascular device position, andendovascular device energy emission level and/or intensity.

The present disclosure can provide a number of advantages depending onthe particular configuration. The endovascular device monitoring systemcan not only detect and provide feedback to the user, such as whetherendovascular device movement is too fast, too slow or just right, butalso regulate endovascular device movement, thereby enabling physiciansto gauge properly endovascular device movement during a procedure andproviding optimal usage of the endovascular device (even forendovascular devices requiring a narrow range of advancement rates foreffective performance). The movement of laser catheters, in particular,can be reliably, consistently, and accurately maintained at a rate ofless than about 1 mm/second, providing a decreased risk of injury(particularly during superior vena cava during lead extraction),decreasing the forces acting at the laser sheath tip, and preventing thelaser from improperly ablating tissue (particularly with a smaller bodylumen diameter with rapid catheter advancement). The endovascular devicemonitoring system can also determine endovascular device distal end ortip position within the patient. This may operate in lieu of orcomplement an imaging system using radiopaque markers on theendovascular device to track endovascular device distal tip position.

These and other advantages will be apparent from the disclosure of theaspects, embodiments, and configurations contained herein.

As used herein, “at least one”, “one or more”, and “and/or” areopen-ended expressions that are both conjunctive and disjunctive inoperation. For example, each of the expressions “at last one of A, B andC”, “at least one of A, B, or C”, “one or more of A, B, and C”, “one ormore of A, B, or C” and “A, B, and/or C” means A alone, B alone, Calone, A and B together, A and C together, B and C together, or A, B andC together. When each one of A, B, and C in the above expressions refersto an element, such as X, Y, and Z, or class of elements, such asX₁-X_(n), Y₁-Y_(m), and Z₁-Z_(o), the phrase is intended to refer to asingle element selected from X, Y, and Z, a combination of elementsselected from the same class (e.g., X₁ and X₂) as well as a combinationof elements selected from two or more classes (e.g., Y₁ and Z_(o)).

It is to be noted that the term “a” or “an” entity refers to one or moreof that entity. As such, the terms “a” (or “an”), “one or more” and “atleast one” can be used interchangeably herein. It is also to be notedthat the terms “comprising”, “including”, and “having” can be usedinterchangeably.

The term “automatic” and variations thereof, as used herein, refers toany process or operation done without material human input when theprocess or operation is performed. However, a process or operation canbe automatic, even though performance of the process or operation usesmaterial or immaterial human input, if the input is received beforeperformance of the process or operation. Human input is deemed to bematerial if such input influences how the process or operation will beperformed. Human input that consents to the performance of the processor operation is not deemed to be “material”.

A “catheter” is a tube that can be inserted into a body cavity, duct,lumen, or vessel. In most uses, a catheter is a thin, flexible tube(“soft” catheter), though in some uses, it is a larger, solid (“hard”)catheter.

The term “computer-readable medium” as used herein refers to any storageand/or transmission medium that participate in providing instructions toa processor for execution. Such a medium is commonly tangible andnon-transient and can take many forms, including but not limited to,non-volatile media, volatile media, and transmission media and includeswithout limitation random access memory (“RAM”), read only memory(“ROM”), and the like. Non-volatile media includes, for example, NVRAM,or magnetic or optical disks. Volatile media includes dynamic memory,such as main memory. Common forms of computer-readable media include,for example, a floppy disk (including without limitation a Bernoullicartridge, ZIP drive JAZ drive), a flexible disk, hard disk, magnetictape or cassettes, or any other magnetic medium, magneto-optical medium,a digital video disk (such as CD-ROM), any other optical medium, punchcards, paper tape, any other physical medium with patterns of holes, aRAM, a PROM, and EPROM, a FLASH-EPROM, a solid state medium like amemory card, any other memory chip or cartridge, a carrier wave asdescribed hereinafter, or any other medium from which a computer canread. A digital file attachment to e-mail or other self-containedinformation archive or set of archives is considered a distributionmedium equivalent to a tangible storage medium. When thecomputer-readable media is configured as a database, it is to beunderstood that the database may be any type of database, such asrelational, hierarchical, object-oriented, and/or the like. Accordingly,the disclosure is considered to include a tangible storage medium ordistribution medium and prior art-recognize equivalents and successormedia, in which the software implementations of the present disclosureare stored. Computer-readable storage medium commonly excludes transientstorage media, particularly electrical, magnetic, electromagnetic,optical, magneto-optical signals.

“Coronary catheterization” is a generally minimally invasive procedureto access the coronary circulation and/or blood filled chambers of theheart using a catheter. It is performed for both diagnostic andinterventional (treatment) purposes.

The terms “determine”, “calculate” and “compute,” and variationsthereof, as used herein, are used interchangeably and include any typeof methodology, process, mathematical operation or technique.

A “lead” is a conductive structure, typical electrically insulatedcoiled wire. The electrically conductive material can be any conductivematerial, with metals and intermetallic alloys common. The outer sheathof insulative material is biocompatible and biostable (e.g.non-dissolving in the body) and generally includes organic materialssuch as polyurethane and polyimide. Lead types include, by way ofnon-limiting example, epicardial and endocardial leads. Leads arecommonly into a body percutaneously or surgically.

The term “means” as used herein shall be given its broadest possibleinterpretation in accordance with 35 Section 112, Paragraph 6Accordingly, a claim incorporating the term “means” shall cover allstructures, materials, or acts set forth herein, and all of theequivalents thereof. Further, the structures, materials or acts and theequivalents thereof shall include all those described in the summary ofthe invention, brief description of the drawings, detailed description,abstract, and claims themselves.

The term “module” as used herein refers to any known or later developedhardware, software, firmware, artificial intelligence, fuzzy logic, orcombination of hardware and software that is capable of performing thefunctionality associated with that element. Also, while the disclosureis presented in terms of exemplary embodiments, it should be appreciatedthat individual aspects of the disclosure can be separately claimed.

A “non-Newtonian fluid” is a fluid whose flow properties differ in anyway from those of Newtonian fluids. Most commonly the viscosity (measureof a fluid's ability to resist gradual deformation by shear or tensilestresses) of non-Newtonian fluids is dependent on shear rate or shearrate history. However, there are some non-Newtonian fluids withshear-independent viscosity, that nonetheless exhibit normalstress-differences or other non-Newtonian behavior. Many salt solutions,suspensions, and molten polymers are non-Newtonian fluids. In aNewtonian fluid, the relation between the shear stress and the shearrate is linear, passing through the origin, the constant ofproportionality being the coefficient of viscosity. In a non-Newtonianfluid, the relation between the shear stress and the shear rate isdifferent, and can even be time-dependent.

“Radio-Frequency IDentification” (RFID) refers to the use of a wirelessnon-contact system that uses radio-frequency electromagnetic fields totransfer data from a tag attached to an object, for the purposes ofautomatic identification and/or tracking. Some tags require no batteryand are powered and read at short ranges via magnetic fields(electromagnetic induction) (known as passive RFID tags). Others use alocal power source and emit radio waves (electromagnetic radiation atradio frequencies) (known as active RFID tags). The tag containselectronically stored information which may be read from up to severalmeters away. Unlike a bar code, the tag does not need to be within lineof sight of the reader and may be embedded in the tracked object.

A “surgical implant” is a medical device manufactured to replace amissing biological structure, support, stimulate, or treat a damagedbiological structure, or enhance, stimulate, or treat an existingbiological structure. Medical implants are man-made devices, in contrastto a transplant, which is a transplanted biomedical tissue. In somecases implants contain electronics, including, without limitation,artificial pacemaker, defibrillator, electrodes, and cochlear implants.Some implants are bioactive, including, without limitation, subcutaneousdrug delivery devices in the form of implantable pills or drug-elutingstems.

It should be understood that every maximum numerical limitation giventhroughout this disclosure is deemed to include each and every lowernumerical limitation as an alternative, as if such lower numericallimitations were expressly written herein. Every minimum numericallimitation given throughout this disclosure is deemed to include eachand every higher numerical limitation as an alternative, as if suchhigher numerical limitations were expressly written herein. Everynumerical range given throughout this disclosure is deemed to includeeach and every narrower numerical range that falls within such broadernumerical range, as if such narrower numerical ranges were all expresslywritten herein.

The preceding is a simplified summary of the disclosure to provide anunderstanding of some aspects of the disclosure. This summary is neitheran extensive nor exhaustive overview of the disclosure and its variousaspects, embodiments, and configurations. It is intended neither toidentify key or critical elements of the disclosure nor to delineate thescope of the disclosure but to present selected concepts of thedisclosure in a simplified form as an introduction to the more detaileddescription presented below. As will be appreciated, other aspects,embodiments, and configurations of the disclosure are possibleutilizing, alone or in combination, one or more of the features setforth above or described in detail below.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings are incorporated into and form a part of thespecification to illustrate several examples of the present disclosure.These drawings, together with the description, explain the principles ofthe disclosure. The drawings simply illustrate preferred and alternativeexamples of how the disclosure can be made and used and are not to beconstrued as limiting the disclosure to only the illustrated anddescribed examples. Further features and advantages will become apparentfrom the following, more detailed, description of the various aspects,embodiments, and configurations of the disclosure, as illustrated by thedrawings referenced below.

FIG. 1 depicts an introducer sheath assembly according to an embodimentof this disclosure;

FIG. 2 depicts a catheter monitoring system according to an embodimentof this disclosure;

FIG. 3 depicts a control algorithm according to an embodiment of thisdisclosure;

FIG. 4 depicts a control algorithm according to an embodiment of thisdisclosure;

FIG. 5 depicts a catheter assembly according to an embodiment of thisdisclosure;

FIG. 6 depicts a catheter assembly according to an embodiment of thisdisclosure;

FIG. 7 depicts a catheter movement sensor according to an embodiment;and

FIG. 8 depicts a catheter movement sensor according to an embodiment.

DETAILED DESCRIPTION

Endovascular device movement is monitored and/or controlled by anendovascular device monitoring system. The endovascular devicemonitoring system is commonly automated to avoid human error. While theendovascular device monitoring system is discussed with specificreference to catheters, it is to be understood that it can apply equallyto other endovascular devices, such as lead removal or extractionsheaths, needles, surgical instruments, snares, and the like. Theendovascular device monitoring system can be used for any type ofcatheter, including without limitation laser ablation, cauterization,and lead removal catheter systems.

FIG. 1 depicts an introducer sheath assembly 100 for monitoring catheterusage according to an embodiment. The introducer sheath assembly 100includes a sheath 104 having a sheath lumen 106, a distal tip 108, andproximal end 112. The proximal end 112 includes a side port 116 in fluidcommunication with a valve 120 and a catheter movement sensor 124. Acatheter (not shown) can be introduced through a main port 128 in thevalve 120 or side port 116. The main port is coaxial with the lumen 106.

FIG. 5 depicts a catheter assembly 500 for monitoring catheter usageaccording to another embodiment. The catheter assembly 500 is positionedsubcutaneously (underneath the skin 502 of a patient) and includes acatheter body 504 and a catheter movement sensor 124. The cathetermovement sensor 124 is an integral part of the subcutaneous portion ofthe introducer sheath assembly.

FIG. 6 depicts a catheter assembly 600 monitoring catheter usageaccording to yet another embodiment. The catheter assembly 600 ispositioned subcutaneously and includes a catheter body 504 and acatheter movement sensor 124. Unlike the catheter assembly 500, thecatheter movement sensor 124 is an integral part of the catheterassembly. The catheter assembly 600 can be a modified version of acoronary laser atherectomy catheter by the Spectranetics Corporationunder the tradenames ELCA™ and Turbo Elite™ (each of which is used forcoronary intervention or catheterization such as recanalizing occludedarteries, changing lesion morphology, and facilitating stent placement)or a laser sheath sold under the tradename SLSII™ and GlideLight™ (whichis used for surgically implanted lead removal).

The catheter movement sensor 124 in any of the above embodiments canhave many different configurations. Velocity, speed, acceleration,and/or position of a catheter can be determined by one or more ofmechanical, optical, ultrasound (acoustic), magnetic, electrical, andelectromagnetic sensing techniques.

FIG. 7 illustrates an example of a mechanical sensing technique. Themechanical movement sensor 700 includes counter-rotating first andsecond wheels 704 a,b engaging a catheter body 504 as it advances orwithdraws from a body lumen. As will be appreciated, the velocity orrate of movement and position of the catheter body 504 are a function ofthe rate of rotation of the first and/or second wheel 704 a,b. Whileposition may be tracked using only one wheel engaging the catheter body504, the frictional forces opposing catheter movement could be higher,thereby creating hindering catheter operation by the physician. Othermechanical techniques will be obvious to those of ordinary skill in theart.

FIG. 8 illustrates an example of a radiation sensing technique in whichthe catheter movement sensor 124 includes not only a detector but alsoone or more markers 804 spaced at predetermined intervals 808 (which maybe equidistant or non-equidistant) along a length of the catheter body800. Adjacent markers may be used to start and stop a timer to measure apredetermined time interval required to transgress the interveningpredetermined interval 808 and counting the transgressed markers todetermine a subcutaneous length or approximate position of the distaltip of the catheter. The markers may be substantially identical orconfigured differently. An example of the latter is where each marker isdetectably encoded (e.g., each marker being configured as a unique orsubstantially unique bar code) to represent a distance from a selectedreference point.

The detector and markers of the catheter movement sensor 124 aretypically located on different ones of the introducer sheath 100 andcatheter itself. For example, the markers can be located on the catheterbody 800 as shown, and the detector on the introducer sheath 100.Alternatively, the marker(s) can be located on the introducer sheath100, and the detector on or in the catheter.

In the case of optical sensing, the markers 804 can be any marker thatreflects light in a detectable and consistent manner. The markers 804typically have an optical property, such as reflectance (orreflectivity), absorbance (or absorption), and the like, different fromthat of the intervening catheter body 800. A light source emitsmodulated or unmodulated light onto the catheter body 800 as the body800 moves. Light reflected along a length of the catheter body 800 iscaptured by the detector typically configured as an array ofphotoelectric devices. The detector dissects the reflected light intoits various spectra. The differing optical properties of the lightreflected by the markers when compared with the intervening body 800 aretranslated into an electric signal, which is output to a controller.

In the case of magnetic sensing, the markers are magnetic or have amagnetic property different from that of the intervening catheter body800. The detector can be a magnetic field sensor, such as a rotatingcoil, Hall effect magnetometer, NMR magnetometer, SQUID magnetometer, orfluxgate magnetometer that can measure variations in magnetic fieldstrength along a length of the catheter body 800 and thereby locate themarkers. The measured magnetic field variations when compared with theintervening body 800 are translated into an electric signal, which isoutput to a controller.

In the case of ultrasonic sensing, the markers have a differentultrasonic transmission property than the intervening catheter body 800.An ultrasound transducer can act both as the ultrasonic emitter anddetector to detect reflected or transmitted ultrasonic energy andthereby locate the markers. An electrical signal is generated when eachmarker passes the detector, which signal is output to a controller.

In the case of sensing using other wavelengths of radiation (such asx-rays), the markers can include a radiopaque material, such as gold orother metal, while the intervening catheter body 800 includes aradiolucent material, or vice versa, such that the markers have adifferent imaging property than the intervening catheter body 800. Anelectrical signal is generated when each marker passes a conventionaldetector, which signal is output to a controller.

In the case of electrical sensing, the markers are electricallyconductive or have an electrical conductivity or resistivity differentfrom that of the intervening catheter body 800. An electrical parameter,such as voltage, current, resistance, or ambient electric field can bedetected to determine marker location. The detector, for example, can bea voltmeter, ammeter, magnetoresistive field sensor, Hall Effect currentsensor transducer, potentiometer, oscilloscope, LCR meter, and the like.An electrical signal is generated when each marker passes the detector,which signal is output to a controller.

An example of sensing using a combination of electromagnetic energy andelectrical sensing is radio-frequency identification. The markers can beconfigured as active or passive RFID tags. In one configuration, themarkers are configured as passive RFID tags, and the detector as anactive or powered RFID reader. In another configuration, the markers areconfigured as active RFID tags, and the detector as an active or passiveRFID reader.

As will be appreciated, the above discussion presents examples only andis not intended to be exhaustive. One of ordinary skill in the art willappreciate that other sensing techniques can be employed depending onthe application.

FIG. 2 depicts a catheter monitoring system 200 according to anembodiment. The catheter monitoring system 200 includes the cathetermovement sensor 124 in signal communication with a controller 204, whichis, in turn, in signal communication with a user interface 208 and acatheter parameter adjustment module 212. The controller 204 executesone or more microprocessor executable control algorithms stored in acomputer readable medium to receive catheter movement signals from thecatheter movement sensor 124 and, based on the received cathetermovement signals, provide alarm and other output to the user via userinterface 208 and/or effect catheter parameter adjustment via thecatheter parameter adjustment module 212. The user interface can provideaudible (e.g., sounds), tactile, and/or visual (e.g., lights) output tothe user and receive user commands as input to the controller 204.Audible, tactile, acid and/or visual output relates to one or more ofcatheter movement and/or catheter distal tip location within the bodylumen. The catheter parameter(s) adjusted by the catheter parameteradjustment module 212 include one or more of catheter velocity,acceleration, speed, operational state (e.g., on or off), catheterenergy emission level or intensity, catheter (distal end) position, andthe like.

Catheter parameter adjustment or regulation can be effected by varioustechniques. Catheter velocity, acceleration, and/or speed can beadjusted by selectively and/or variably increasing resistance tocatheter movement, such as by hydraulic resistance applied to thecatheter or a part thereof, frictional resistance applied to thecatheter or a part thereof by a braking system, resistance posed bymovement of the catheter or a part thereof through a non-Newtonian fluid(such as Dilitant), resistance created by movement of a magneticmaterial associated with the catheter through an external magnetic field(which may be from a magnet or flow of charged particles), and othermeans of slowing, or retarding catheter movement. Catheter operationalstate can be controlled or regulated by turning an energy emitter in thecatheter on or off, catheter energy emission level or intensity can becontrolled or regulated by altering a degree of energization of a powersource of the energy emitter.

An operation of the controller 204 will now be described with referenceto FIG. 3.

Operation commences when the controller 204 senses a stimulus in step300. The stimulus, for example, can be receipt of user input, receipt ofa catheter movement signal from the catheter movement sensor 124,passage of time, and the like.

In step 304, the controller 204 selects a spatial increment over whichto determine catheter velocity, acceleration, and/or speed and, ifnecessary, a reference location at which to detect, track or otherwiseobserve marker movement. A typical selected spatial increment is thespatial interval between adjacent markers 804, though the selectedspatial increment can span more than two increments depending on theapplication. Differently sized spatial intervals can be selected fordifferent types of procedures and/or catheters. Typically, the referencelocation is the location of the catheter movement sensor 124 or acomponent thereof.

In step 308, the controller 204 determines the time interval requiredfor the catheter to traverse the selected spatial increment. The timeinterval can be determined, for example, by initiating or reading astart time on a timer (not shown) when a first marker passes a detectorand terminating or reading a stop time on the timer when the markerassociated with the end of the selected spatial increment passes thedetector.

In optional step 312, the controller 204 determines a catheter movementrate (e.g., velocity, acceleration, and/or speed) and/or distal tipposition (based on the number of markers that have transgressed thedetector). Depending on the application, this step may be unnecessarywhere the time interval is mapped directly to a lookup table showingacceptable and unacceptable time intervals and/or the number oftransgressed markers is mapped directly to the subcutaneous length orthe catheter and therefore the approximate catheter distal tip position.

In step 316, the controller 204 retrieves predetermined cathetermovement and/or catheter distal tip position thresholds. Thepredetermined thresholds can have a corresponding rule regarding aresponse if the predetermined threshold is triggered. The rule, forexample, can be to provide audible, tactile, and/or visual output to theuser, alter a catheter parameter, and/or regulate a catheter movementrate.

In decision diamond 320, the controller 204 determines, based on acomparison of a predetermined threshold to the determined cathetermovement rate and/or determined time interval and/or catheter distal tipposition, whether catheter movement and/or position is/are acceptable.When acceptable, the controller 204 proceeds to step 324 and optionallynotifies the user accordingly. When unacceptable, controller 204proceeds to step 328 and initiates a warning to the user and/oralters/controls one or more catheter parameters as described previously.After completing steps 324 and 328, the controller 204 returns to andrepeats step 308.

A further operation of the controller 204 will now be described withreference to FIG. 4. The operation is based on user selection between anassisted and unassisted mode of operation. The assisted mode ofoperation enables the controller not only to provide audible, tactile,and/or visual feedback to the user but also regulate one or morecatheter parameters. The unassisted mode of operation enables thecontroller to provide audible, tactile, and/or visual feedback to theuser but not to regulate one or more catheter parameters.

In step 400, the controller 204 senses a stimulus, including thoseindicated above.

In step 404, the controller 204 determines a current mode of operation.the current mode of operation is typically selected by the user but candefault to an assisted mode when catheter operation is unacceptable.

In step 408, the controller 204 determines that the current operatingmode is the assisted mode and, in response, controls a rate of catheteradvancement or removal using any of the techniques noted above.

In step 412, the controller 204 determines that the current operatingmode is the unassisted mode and, in response, monitors the rate ofcatheter advancement or removal and provides appropriate audible,tactile, and/or visual output to the user.

A number of variations and modifications of the disclosure can be used.It would be possible to provide for some features of the disclosurewithout providing others.

For example in one alternative embodiment, the teachings of thisdisclosure are used with an unpowered catheter mounting any one or moreof a variety of tools, such as dilation balloons, cutting balloons,cutting blades, drug release mechanisms, imaging devices, blood flowsensors, contrast media, and the like.

The present disclosure, in various aspects, embodiments, andconfigurations, includes components, methods, processes, systems and/orapparatus substantially as depicted and described herein, includingvarious aspects, embodiments, configurations, subcombinations, andsubsets thereof. Those of skill in the art will understand how to makeand use the various aspects, aspects, embodiments, and configurations,after understanding the present disclosure. The present disclosure, invarious aspects, embodiments, and configurations, includes providingdevices and processes in the absence of items not depicted and/ordescribed herein or in various aspects, embodiments, and configurationshereof, including in the absence of such items as may have been used inprevious devices or processes, e.g., for improving performance,achieving ease and or reducing cost of implementation.

The foregoing discussion of the disclosure has been presented forpurposes of illustration and description. The foregoing is not intendedto limit the disclosure to the form or forms disclosed herein. In theforegoing Detailed Description for example, various features of thedisclosure are grouped together in one or more, aspects, embodiments,and configurations for the purpose of streamlining the disclosure. Thefeatures of the aspects, embodiments, and configurations of thedisclosure may be combined in alternate aspects, embodiments, andconfigurations other than those discussed above. This method ofdisclosure is not to be interpreted as reflecting an intention that theclaimed disclosure requires more features than are expressly recited ineach claim. Rather, as the following claims reflect, inventive aspectslie in less than all features of a single foregoing disclosed aspects,embodiments, and configurations. Thus, the following claims are herebyincorporated into this Detailed Description, with each claim standing onits own as a separate preferred embodiment of the disclosure.

Moreover, though the description of the disclosure has included thedescription of one or more aspects, embodiments, or configurations andcertain variations and modifications, other variations, combinations,and modifications are within the scope of the disclosure, e.g., as maybe within the skill and knowledge of those in the art, afterunderstanding the present disclosure. It is intended to obtain rightswhich include alternative aspects, embodiments, and configurations tothe extent permitted, including alternate, interchangeable and/orequivalent structures, functions, ranges or steps to those claimed,whether or not such alternate, interchangeable and or equivalentstructures, functions, ranges or steps are disclosed herein, and withoutintending to publicly dedicate any patentable subject matter.

1. A method, comprising: determining, by a microprocessor executablecontroller and based on movement of an endovascular device past aselected reference location, at least one of a movement rate of anendovascular device and position of a distal end of an endovasculardevice in a body of a patient. 2-30. (canceled)